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(A) AS patient with 15q11-13. (B) AS patient with uniparental disomy. (C) AS patient with imprinting defect. (D) AS patient with UBE3A mutation. | Clayton-Smith, J., & Laan, L. (2003). Angelman syndrome: a review of the clinical and genetic aspects. Journal of Medical Genetics, 40(2), 87 LP-95. https://doi.org/10.1136/jmg.40.2.87

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